Pruradik (crotamiton) NDC 73352-051

NDC codes

FDA NDC Directory

Product NDC (as listed)73352-051Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73352-0051Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
73352-051-10	73352005110	237 g in 1 BOTTLE, PLASTIC (73352-051-10)Marketed from Jun 2, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Pruradik
Generic name (nonproprietary): crotamiton
Active ingredients: Crotamiton — 100 mg/g
Dosage form: Lotion
Route: Topical
Labeler: Trifluent Pharma, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 087204
Marketing start: Jun 2, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 73352-051_36991086-14b5-9e66-e063-6394a90ad654SPL ID 36991086-14b5-9e66-e063-6394a90ad654SPL set ID 3699175f-bfc8-a047-e063-6394a90a80d1RxCUI 106219UNII D6S4O4XD0HUPC 0373352051106

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473352005110 followed by a unit qualifier and the quantity

Package 73352-0051-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 087204

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 087204
Product	Strength	Form · route	Labeler	Product NDC
Crotancrotamiton	Crotamiton 100 mg/g	LotionTopical	Marnel Pharmaceuticals, Inc.	0682-0051